Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 48
Page 73
Product of first reduction step of reasurin . Therefore , no specific tolerances for
Eh can be set ... will oxygen per cell in many bacterial cultures . This increase by
30 to 60 mV per pH unit of decrease illustrates the importance of creating
reducing ...
Product of first reduction step of reasurin . Therefore , no specific tolerances for
Eh can be set ... will oxygen per cell in many bacterial cultures . This increase by
30 to 60 mV per pH unit of decrease illustrates the importance of creating
reducing ...
Page 74
Reducing agents for anaerobic media completely oxidized ( its use will be
described along with other reducing agents below ) . Compounds ( mV ) Concn
in media 6 . 6 . 2 . Reducing Agents < - 100 - 210 ( 22 ) - 330 ( 22 ) - 420 0 . 05 %
0 .
Reducing agents for anaerobic media completely oxidized ( its use will be
described along with other reducing agents below ) . Compounds ( mV ) Concn
in media 6 . 6 . 2 . Reducing Agents < - 100 - 210 ( 22 ) - 330 ( 22 ) - 420 0 . 05 %
0 .
Page 441
These two articles provide extensive practical information for performance of the
acetylene reduction technique under both laboratory and field conditions . The
chromatographic analysis of ethylene and the various factors affecting acetylene
...
These two articles provide extensive practical information for performance of the
acetylene reduction technique under both laboratory and field conditions . The
chromatographic analysis of ethylene and the various factors affecting acetylene
...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
Copyright | |
25 other sections not shown
Other editions - View all
Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino acids amount anaerobic applications appropriate assay autoclaving bacteria Bacteriol base broth buffer cells centrifuge colonies column components compounds concentration containing counting cover culture described determine dilution Dissolve distilled water effective electron enzyme example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts sample selection separation slide sodium solution specific staining standard sterile substrate surface suspension Table techniques temperature tion transfer tube usually values vitamin volume Wash York